US647280A - Process of producing indigo. - Google Patents
Process of producing indigo. Download PDFInfo
- Publication number
- US647280A US647280A US73950799A US1899739507A US647280A US 647280 A US647280 A US 647280A US 73950799 A US73950799 A US 73950799A US 1899739507 A US1899739507 A US 1899739507A US 647280 A US647280 A US 647280A
- Authority
- US
- United States
- Prior art keywords
- indigo
- isatin
- alpha
- red
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 235000000177 Indigofera tinctoria Nutrition 0.000 title description 12
- 229940097275 indigo Drugs 0.000 title description 12
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 title description 12
- 238000000034 method Methods 0.000 title description 4
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 8
- CRDNMYFJWFXOCH-BUHFOSPRSA-N Couroupitine B Natural products N\1C2=CC=CC=C2C(=O)C/1=C1/C2=CC=CC=C2NC1=O CRDNMYFJWFXOCH-BUHFOSPRSA-N 0.000 description 6
- CRDNMYFJWFXOCH-UHFFFAOYSA-N indirubin Chemical compound N1C2=CC=CC=C2C(=O)C1=C1C2=CC=CC=C2NC1=O CRDNMYFJWFXOCH-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- UYJXRRSPUVSSMN-UHFFFAOYSA-P ammonium sulfide Chemical compound [NH4+].[NH4+].[S-2] UYJXRRSPUVSSMN-UHFFFAOYSA-P 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ZGPFGHSOYPBCGI-UHFFFAOYSA-N 1-chloroindole-2,3-dione Chemical compound C1=CC=C2N(Cl)C(=O)C(=O)C2=C1 ZGPFGHSOYPBCGI-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B7/00—Indigoid dyes
- C09B7/02—Bis-indole indigos
Definitions
- the alcohol may be substituted by Water, benzol, 8m. 5 What I claim as new, and desire to secure by Letters Patent, is-
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Description
UNITED STATES PATENT OFFICE.
TRAUGOTT SANDMEYER, OF IBASLE, SWITZERLAND,ASSIGNOR TO JOHN R.
GEIGY & 00., OF SAME PLACE.
PROCESS OF PRODUCING INDIGO.
SPECIFICATION forming part of Letters Patent N 0. 647,280, dated April 10, 1900.
Application filed December 7, 1899. Serial No. 739,507. (No Specimens.)
To all whom it may concern.-
Be itknown that I, TRAUGOTT SANDMEYER, a citizen of the Swiss Confederation, residing at Basic, Switzerland, have invented certain new and useful Improvements in Processes of Making Indigo, Pure and Mixed with Indigo- Red, of which the following is a specification.
Ad. Von Baeyer has proved in his fundamental works on indigo that certain derivatives of isatin-as, for instance, isatin chlorid, the pseudoisatin -alpha-oxim, and the ethers of isatin-by moderate reduction can be transformed, particularly with ammonium sulfid, into indigo, with which, however, always more or less indigo-red is formed, (Berichte den Deu/tschen Ohemischen Gescllschctfz, Vol. XI, p. 1217; XII, 4:56; XVI, 2203.)
In my application, Serial No. 739,508, filed December 7, 1899, I have described the production of a new derivative of isatin-namely, alpha-isatin-anilidof the formula:
i beta/ 3 :0
or in the tautomeric pseudoform NH \alpha o=Nc,H, beta/ rivatives, but in practical working with the very important difference that the formation of indigo from the pure substance takes place very easily and nearly without any admixture of indigo-red. However, such an admixture of indigo-red can be brought about in every desirable proportion if the reduction of the alpha-isatin-anilid is carried out in the presence of certain quantities of isatin. The ammonium sulfid which Ad. vou Baeyer has employed with success has also proved to be in this case the most suitable reducing agent.
The following examples will serve to illus trate the manner in which the invention can be carried into practical eifect. The parts are by weight:
Earctmple IProcluczion of indzIgo.To a warm solution of twenty parts of alpha-isatinanilid in sixty parts of alcohol are quickly added, with stirring, forty parts of a freshlyprepared solution of ammonium sulfid c011- taining ten per cent. of sulfureted hydrogen. By the chemical heat of the reaction the so lution turns in color to green and then to blue,
and the immediate separation of indigo inv small crystals takes place. Finally, the mix ture is boiled for a short time, and then the indigo is filtered off, Washed with hot alcohol, and dried. The sulfur it contains can be removed by treatment with carbon disulfid.
Eacctmple II-Producti0n of determinate mixtures of indigo and ind1Yqo-red.To' a warm solution of five parts of isatin and fifteen parts of alpha-isatin-anilid in sixty parts of alcohol are quickly added, with stirring, forty parts of the above (example I) mentioned solution of ammonium sulfid. The separation of the mixture of indigo with indigo-red takes place in the same way, and the further treatment is the same as that above described, Example I. In appearance the product differs little from the foregoing one. Both are dark crystalline powders showing a slight copper-colored luster; but their dyeings, also the solution of their sulfonic acids, show a surprising difference in the shades, which, according to the employed quantity of isatin,
vary from the greenish blue of pure indigo earmine to reddish violet.
In these examples the alcohol may be substituted by Water, benzol, 8m. 5 What I claim as new, and desire to secure by Letters Patent, is-
The herein-described process of producing v indigo pure and mixed with indigo-red, which consists in forming a suitable solution of alpha-isatin-anilid of the formula:
01- in the tautomeric pseudoform In testimony that I claim the foregoing as my invention I have signed my name in presence of two subscribing witnesses.
TRAUGOTT SANDMEYER.
Witnesses:
GEORGE GIFEoRD, ALBERT GRAETER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73950799A US647280A (en) | 1899-12-07 | 1899-12-07 | Process of producing indigo. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73950799A US647280A (en) | 1899-12-07 | 1899-12-07 | Process of producing indigo. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US647280A true US647280A (en) | 1900-04-10 |
Family
ID=2715853
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US73950799A Expired - Lifetime US647280A (en) | 1899-12-07 | 1899-12-07 | Process of producing indigo. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US647280A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050241159A1 (en) * | 2002-08-02 | 2005-11-03 | Koninkilijke Phillips Electronics N.V. | Wear-resistant stainless cutting element of an electric shaver, electric shaver, and method of producing such a cutting element |
| WO2018100277A1 (en) | 2016-12-01 | 2018-06-07 | Provepharm Life Solutions | Process for preparing indigo carmine |
-
1899
- 1899-12-07 US US73950799A patent/US647280A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050241159A1 (en) * | 2002-08-02 | 2005-11-03 | Koninkilijke Phillips Electronics N.V. | Wear-resistant stainless cutting element of an electric shaver, electric shaver, and method of producing such a cutting element |
| WO2018100277A1 (en) | 2016-12-01 | 2018-06-07 | Provepharm Life Solutions | Process for preparing indigo carmine |
| US10767054B2 (en) | 2016-12-01 | 2020-09-08 | Provepharm Life Solutions | Process for preparing indigo carmine |
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